Reported Sep 25, 2024 · Ongoing
Alaris Syringe Module Model 8110, a modular infusion pump and monitoring system
CareFusion 303, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: CareFusion 303, Inc. · 10020 Pacific Mesa Blvd · San Diego, CA · 92121-4386
Is this the product you have?
- Alaris Syringe Module Model 8110, a modular infusion pump and monitoring system
- Lot codes and dates
- Model Number8110
- UDI-DI codes
108854035160471088540351532310885403811043108854038110361088540381101210885403424267
- Serial Numbers16
3,606 of 3,606 codes
165575171655752316558377165580301655755316552258165582591655576716557678165579411655770616557760162014781620410416201486162070891620418116201491162015521620690616203916162014841620154616203885162016161620714516201496162016111620632716204189162039591620682716204092162069371620684316201523162015561620638116206138162041291620579416204207162011661620149316204172162015171620156416204027162064731620721116204173162037331620691516206904162014801620148916201498162016231620148116201163
- Amount recalled
- 20145
This recall covers 5 products
The agency filed one notice per product. You are reading one of them; the other 4 are below.
Where it was sold
Why it was recalled
Due to affected devices that may have bent female IUI connector and may not be operable and potentially cause delays in the start of the infusion or monitoring.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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